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NCT Number: NCT05716880

Ketoanalogues for Muscle Mass Loss in Nephrotic Syndrome

The goal of this non-commercial clinical trial is to assess efficacy and safety of ketoanalogues of essential amino acids in the prevention of protein-energy wasting in nephrotic syndrome.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Department of Internal Diseases, Nephrology and Dialysis, Military Institute of Medicine - National Research Institute

Warsaw, Masovian District, 04-141, Poland

Location status: Recruiting

Location contact

Anna Matyjek, MD, PhD

CONTACT

[email protected]

261817045 ext. +48

Stanislaw Niemczyk, MD, PhD, Prof.

PRINCIPAL_INVESTIGATOR

About this study

Adult patients with new diagnosis or relapse of nephrotic syndrome and glomerular filtration rate of ≥ 30 mL/min/1.73m2 will be included in the study. Exclusion criteria will be a secondary cause of nephrotic syndrome, morbid obesity and severe diseases affecting nutritional status.

Participants will be randomly assigned to the intervention group (KA+MPD) or control group (MPD); randomization will be stratified by type of glomerular disease (podocytopathy or other type) and investigational site. The control group will follow the diet recommended in nephrotic syndrome - a medium protein diet (MPD) - under the care of a dietitian. Intervention group will receive Ketosteril (1 tablet for every 5 kg of ideal body weight) as an addition to the diet. All patients will also receive treatment for underlying glomerular disease in accordance with current guidelines and local practice.

The main objective is to assess the efficacy of Ketosteril as an add-on therapy in preventing the loss of lean tissue mass (LTM) over 6 months compared to a standard diet.

The additional aims include the assessment of muscle function parameters, nephrotic syndrome severity and laboratory indicators of catabolism.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Nephrotic syndrome with serum albumin < 3.0 g/dL and daily proteinuria of > 3.5 g/day or > 50 mg/kg;
  • New diagnosis or relapse of nephrotic syndrome (defined as: proteinuria of < 2.0 g/day or uPCR < 2000 mg/g in the last 6 months prior to relapse and prednison dose equal to or less than 10 mg/day in the last 3 months prior relapse);
  • Glomerular filtration rate qual to or higher than 30 mL/min/1.73m2 based on Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equation.

Exclusion criteria

  • Diabetic kidney disease;
  • Small vessels vasculitis;
  • Systemic lupus erythematosus;
  • Positive antinuclear antibodies, anti-dsDNA or antineutrophil cytoplasmic antibodies (ANCA);
  • Positive anti-HIV or anti-hepatitis C antibodies, HBsAg;
  • HbA1c >7%;
  • Monoclonal gammopathy;
  • Pregnancy;
  • Body mass index >= 40 kg/m2;
  • Severe acute or chronic disease affecting nutritional status;
  • Neoplasm;
  • Contraindication to Ketosteril;
  • Alcohol or drug abuse;
  • Mental disorders;
  • Failure to comply with medical recommendations, lack of cooperation;
  • Participation in other clinical trial or the use of Ketosteril in the last 1 year prior to screening.

Treatment and study plan

Ketosteril

Drug

Daily dose = 1 tabl / 5 kg of ideal body weight

Medium Protein Diet (MPD)

Other

MPD: daily protein intake of 0.8-1.0 g/kg of ideal body weight + up to 5 g based on daily proteinuria

Primary outcomes

  1. Maximum loss of lean tissue mass

    Time frame: 6 months

    The difference between the initial lean tissue mass (LTM) and the lowest LTM measured within 6 months, expressed in percentage. The non-inferiority hypothesis of Ketosteril use will be tested as the primary endpoint.

    LTM will be measured with bioimpedance spectroscopy.

Secondary outcomes

  1. Maximum loss of lean tissue mass

    Time frame: 6 months

    The difference between the initial lean tissue mass (LTM) and the lowest LTM measured within 6 months, expressed in percentage. The superiority hypothesis of Ketosteril use will be tested as the secondary endpoint.

  2. Neph-PEW diagnosis

    Time frame: 6 months

    The percentage of patients meeting criteria of nephrotic syndrome-associated protein-energy wasting (neph-PEW): reduction of LTM by 3% within 3 months or by 5% within 6 months.

  3. 6-minute walk test distance

    Time frame: 6 months

    Change in distance walked in the 6-minute walk test from baseline value; expressed in meters.

  4. Handgrip strength (HGS)

    Time frame: 6 months

    Change in HGS value from baseline; expressed in kg.

  5. Serum albumin

    Time frame: 6 months

    Change in serum albumin level from baseline value; expressed in g/dL.

  6. Urinary protein/creatinine ratio (uPCR)

    Time frame: 6 months

    Change in uPCR value from baseline; expressed in mg/g.

  7. Low density lipoprotein (LDL)

    Time frame: 6 months

    Change in serum LDL level from baseline; expressed in mg/dL.

  8. Triglycerides

    Time frame: 6 months

    Change in serum triglycerides level from baseline; expressed in mg/dL.

  9. Uric acid

    Time frame: 6 months

    Change in serum uric acid level from baseline; expressed in mg/dL.

  10. Unfavorable disease course

    Time frame: 12 months

    The percentage of patients who experienced the unfavorable disease course including: glomerular disease related death; venous or arterial thromboembolic event; infection requiring hospital admission; acute kidney injury in the stage 2 or 3; sustained glomerular filtration rate reduction over 50% or initiation of kidney replacement therapy; unplanned hospital admission due to complications of nephrotic syndrome treatment.

  11. Glomerular filtration rate

    Time frame: 12 months

    Change in glomerular filtration rate from baseline; expressed in mL/min/1.73m2.

Study contacts

Contact information is provided by the study sponsor or research team.

Anna Matyjek, MD, PhD

CONTACT

[email protected]

261817045 ext. +48

Sponsors and collaborators

Lead sponsor

Military Institute od Medicine National Research Institute

Other

Collaborators

  • Medical University of Lodz
  • Medical University of Warsaw

Registry information

Official study title

FORMA - a Multicenter Randomized-controlled Trial to Evaluate the Efficacy and Safety of Ketoanalogues of Essential Amino Acids in Prophylaxis of Protein-energy Wasting in Nephrotic Syndrome

Acronym: FORMA

Important dates

Study start
2023
Primary completion
2027
Study completion
2027
First posted
Feb 8, 2023
Registry last updated
Feb 8, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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